Rat GRO alpha/CXCL1 (Growth Regulated Oncogene Alpha) ELISA Kit
The Rat GROα/CXCL1 (Growth Regulated Oncogene Alpha) ELISA Kit is a specialized assay designed for the quantitative detection of GROα/CXCL1 levels in rat biological samples. GROα, also known as CXCL1, belongs to the CXC chemokine family and plays a vital role in immune responses, inflammation, and cancer development. This ELISA kit offers exceptional sensitivity and specificity, allowing precise measurement of GROα/CXCL1 concentrations in rat samples. The accurate detection of GROα/CXCL1 is crucial for research focusing on inflammatory responses, tumor microenvironments, and immune regulation, providing valuable insights into various pathological conditions. Manufactured under stringent quality control standards, this ELISA kit ensures robust performance, reliable results, and ease of use, making it an excellent choice for researchers investigating the functions and therapeutic implications of GROα/CXCL1 in biological systems.
Product Name:
Rat GRO alpha/CXCL1 (Growth Regulated Oncogene Alpha) ELISA Kit
SKU:
AEES00287
Size:
96 Assays
Detection Method:
Colorimetric method, ELISA, Sandwich
Assay type:
Sandwich-ELISA
Assay time:
3 h 30 min
Sensitivity:
9.38 pg/mL
Detection range:
15.63-1000 pg/mL
Reovery:
80%-120%
This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to the target protein. Standards or samples are added to the micro ELISA plate wells and bind to the immobilized antibody. A biotinylated detection antibody specific to the target protein is then added, followed by Avidin-Horseradish Peroxidase (HRP) conjugate. Free components are washed away. The substrate solution is added to each well, resulting in a color change. Only wells containing the target protein, detection antibody, and HRP conjugate will develop a blue color. The reaction is terminated by the addition of stop solution, resulting in a yellow color. The optical density (OD) is measured at 450 nm ± 2 nm. The OD value is directly proportional to the concentration of the target protein in the sample and is determined using a standard curve.
